Comparative electrochemical study of some cobalt(III) and cobalt(II) complexes with azamacrocyles and β-diketonato ligands

The electrochemical properties of eight mixed-ligand cobalt(III) and co balt(II) complexes of the general formulas [CoIII(Rac)cyclam (ClO4)2 (1)?(4) and [Co2II(Rac)tpmc](ClO4)3 (5)?(8) were studied. The substances were investigated in aqueous NaClO4 solution and non-aqueous LiClO4/CH3CN solution by cyclic voltam metry at a glassy carbon electrode. In aqueous solution, cyclam and Rac ligands being soluble in water undergo anodic oxidation. Coordination to Co(III) in complexes 1?4, stabilizes these ligands but reversible peaks in catohodic region indicate the redox reaction CoIII/CoII ion. In the case of the binuclear Co(II) complexes 5?8, peaks recorded on the CVs represent oxidation of the bridged Rac ligand. The complexes examined influence the cathodic reaction of hydrogen evolution in aqueous solutions by shifting its potential to more negative values and its current is increased. In non-aqueous solution the CVs of the ligands show irreversible anodic peaks for cyclam, tpmc and for the Rac ligands soluble in acetonitrile. The absence of any peaks in the case of the investigated complexes 1?4 indicates that coordination to Co(III) stabilizes both the cyclam and Rac ligands. Cyclic voltammograms of the complexes 5?8 show oxidation processes of the Rac ligand and Co(II) ions but the absence of a highly anodic peak of the coordinated macrocycle tpmc shows its stabilization. Contrary to in aqueous solution, the redox reaction Co(III)/Co(II) does not occur in acetonitrate indicating a higher stability of the complexes 1?4 in this media in comparison with the binuclear cobalt(II)-tpmc complexes 5?8.